Olanow C W
Department of Neurology, University of South Florida, Tampa.
J Neural Transm Gen Sect. 1993;91(2-3):161-80. doi: 10.1007/BF01245230.
The desire to introduce neuroprotective therapy for Parkinson's disease has begun to focus attention on pathogenetic mechanisms responsible for cell death. Considerable theory and some evidence have now accumulated to suggest that factors related to oxidative stress, mitochondrial bioenergetic defects, excitatory neurotoxicity, calcium cytotoxicity, and trophic factor deficiencies acting either singularly or in combination may contribute to the development of cell death in Parkinson's disease. A better understanding of the specific pathogenetic mechanism involved in cell degeneration might provide a scientific basis for testing a putative neuroprotective therapy. This chapter reviews the theory and evidence in support of these different mechanisms and possible strategies that might provide neuroprotection and interfere with the natural progression of Parkinson's disease.
为帕金森病引入神经保护疗法的愿望已开始将注意力集中在导致细胞死亡的发病机制上。目前已经积累了大量的理论和一些证据,表明与氧化应激、线粒体生物能量缺陷、兴奋性神经毒性、钙细胞毒性以及营养因子缺乏相关的因素,单独或共同作用,可能促成帕金森病中细胞死亡的发生。更好地理解细胞变性所涉及的具体发病机制,可能为测试一种假定的神经保护疗法提供科学依据。本章回顾了支持这些不同机制的理论和证据,以及可能提供神经保护并干预帕金森病自然病程的策略。